ES2229591T3 - Composiciones polimericas biodegradables que comprenden almidon y un polimero termoplastico. - Google Patents

Composiciones polimericas biodegradables que comprenden almidon y un polimero termoplastico.

Info

Publication number: ES2229591T3
Authority: ES; Spain
Prior art keywords: compositions; starch; polyester; acid; compositions according
Prior art date: 1996-11-05
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

ES99113033T

Other languages

English (en)

Spanish (es)

Inventor

Catia Bastioli

Vittorio Bellotti

Gian Domenico Cella

Luciano Del Giudice

Sandro Montino

Gabriele Perego

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Novamont SpA

Original Assignee

Novamont SpA

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1996-11-05

Filing date

1997-11-05

Publication date

2005-04-16

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26332335&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ES2229591(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-11-05 Priority claimed from IT96TO000890 external-priority patent/IT1288817B1/it

1996-12-09 Priority claimed from IT96TO000996 external-priority patent/IT1289723B1/it

1997-11-05 Application filed by Novamont SpA filed Critical Novamont SpA

2005-04-16 Application granted granted Critical

2005-04-16 Publication of ES2229591T3 publication Critical patent/ES2229591T3/es

2017-11-05 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

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238000002156 mixing Methods 0.000 claims abstract description 18
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Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Manufacturing & Machinery (AREA)
Materials Engineering (AREA)
Compositions Of Macromolecular Compounds (AREA)
Biological Depolymerization Polymers (AREA)
Manufacture Of Macromolecular Shaped Articles (AREA)
Polysaccharides And Polysaccharide Derivatives (AREA)
Polyurethanes Or Polyureas (AREA)

ES99113033T 1996-11-05 1997-11-05 Composiciones polimericas biodegradables que comprenden almidon y un polimero termoplastico. Expired - Lifetime ES2229591T3 (es)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
IT96TO000890 IT1288817B1 (it)	1996-11-05	1996-11-05	Composizioni polimeriche eterofasiche comprendenti amido e un polimero termoplastico.
ITTO960890		1996-11-05
IT96TO000996 IT1289723B1 (it)	1996-12-09	1996-12-09	Composizioni polimeriche eterofasiche comprendenti amido e un polimero termoplastico
ITTO960996		1996-12-09

Publications (1)

Publication Number	Publication Date
ES2229591T3 true ES2229591T3 (es)	2005-04-16

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ID=26332335

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Application Number	Title	Priority Date	Filing Date
ES99113033T Expired - Lifetime ES2229591T3 (es)	1996-11-05	1997-11-05	Composiciones polimericas biodegradables que comprenden almidon y un polimero termoplastico.

Country Status (16)

Country	Link
US (3)	US7176251B1 (fr)
EP (6)	EP0950689B1 (fr)
JP (3)	JP4034357B2 (fr)
KR (1)	KR100329588B1 (fr)
CN (1)	CN1104467C (fr)
AT (4)	ATE277124T1 (fr)
AU (1)	AU724397B2 (fr)
BR (1)	BR9712882A (fr)
CA (1)	CA2270362C (fr)
DE (4)	DE69730852T2 (fr)
DK (2)	DK0947559T3 (fr)
ES (1)	ES2229591T3 (fr)
HU (1)	HU229197B1 (fr)
IL (3)	IL129745A0 (fr)
NO (1)	NO335963B1 (fr)
WO (1)	WO1998020073A2 (fr)

Families Citing this family (148)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0950689B1 (fr) *	1996-11-05	2004-10-06	NOVAMONT S.p.A.	Compositions polymériques biodégradables contenant de l'amidon et un polymère thermoplastique
ITTO980524A1 (it) *	1998-06-17	1999-12-17	Novamont Spa	Composizioni contenenti amido aventi elevata resistenza all'invecchiam ento.
IT1305576B1 (it) *	1998-09-22	2001-05-09	Novamont Spa	Polimeri a carattere idrofobico caricati con complessi dell'amido.
WO2000032029A1 (fr) *	1998-12-01	2000-06-08	Garrett Walsh	Fixation de mottes
US6274182B1 (en) *	1999-11-19	2001-08-14	Tfh Publications, Inc.	Animal chew
DE10010826A1 (de)	2000-03-08	2001-09-13	Basf Ag	Verfahren zur Reduktion der Wasserdampfpermeabilität von Folien oder Beschichtungen
US7077994B2 (en) †	2001-10-19	2006-07-18	The Procter & Gamble Company	Polyhydroxyalkanoate copolymer/starch compositions for laminates and films
CN1164661C (zh) *	2001-12-17	2004-09-01	武汉华丽环保科技有限公司	一种淀粉基生物全降解材料及其制备方法
ITMI20020506A1 (it) *	2002-03-11	2003-09-11	Tenax Spa	Procedimento per la realizzazione di elementi lastriformi in materia plastica in particolare reti e simili
US7776314B2 (en)	2002-06-17	2010-08-17	Grunenthal Gmbh	Abuse-proofed dosage system
KR100488438B1 (ko) *	2002-07-15	2005-05-11	이승섭	자체 분해성이 우수한 일회용 프라스틱용기 조성물
DE10258227A1 (de) *	2002-12-09	2004-07-15	Biop Biopolymer Technologies Ag	Biologisch abbaubare Mehrschichtfolie
DE102004032051A1 (de) *	2004-07-01	2006-01-19	Grünenthal GmbH	Verfahren zur Herstellung einer gegen Missbrauch gesicherten, festen Darreichungsform
US8075872B2 (en)	2003-08-06	2011-12-13	Gruenenthal Gmbh	Abuse-proofed dosage form
DE10336400A1 (de)	2003-08-06	2005-03-24	Grünenthal GmbH	Gegen Missbrauch gesicherte Darreichungsform
US20070048228A1 (en) *	2003-08-06	2007-03-01	Elisabeth Arkenau-Maric	Abuse-proofed dosage form
ES2289542T3 (es) *	2003-08-06	2008-02-01	Grunenthal Gmbh	Forma farmaceutica protegida contra un posible abuso.
DE102004020220A1 (de) *	2004-04-22	2005-11-10	Grünenthal GmbH	Verfahren zur Herstellung einer gegen Missbrauch gesicherten, festen Darreichungsform
DE102005005446A1 (de) *	2005-02-04	2006-08-10	Grünenthal GmbH	Bruchfeste Darreichungsformen mit retardierter Freisetzung
DE10361596A1 (de) *	2003-12-24	2005-09-29	Grünenthal GmbH	Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
WO2005052056A1 (fr) *	2003-11-25	2005-06-09	Asahi Kasei Life & Living Corporation	Film mat
US20080036115A1 (en) *	2004-03-10	2008-02-14	Minoru Ueda	Starch Resin Composition, Molded Product Using the Same and Method for Producing the Same
DE102004032103A1 (de) *	2004-07-01	2006-01-19	Grünenthal GmbH	Gegen Missbrauch gesicherte, orale Darreichungsform
DE102004032049A1 (de)	2004-07-01	2006-01-19	Grünenthal GmbH	Gegen Missbrauch gesicherte, orale Darreichungsform
KR20070084032A (ko) *	2004-10-05	2007-08-24	플랜틱 테크놀로지스 리미티드	성형가능한 생분해성 폴리머
CN101360783B (zh) *	2004-10-18	2011-04-06	普朗蒂克科技有限公司	阻透膜
US8802754B2 (en) *	2005-01-25	2014-08-12	Mgpi Processing, Inc.	Starch-plastic composite resins and profiles made by extrusion
DE102005005449A1 (de) *	2005-02-04	2006-08-10	Grünenthal GmbH	Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
CN100497458C (zh) *	2005-02-06	2009-06-10	北京金宝帝生物环保科技有限公司	一种可生物降解的淀粉基高分子组合物、由其制得的薄膜，及其制备方法
ITMI20050452A1 (it)	2005-03-18	2006-09-19	Novamont Spa	Poliestere biodegradabile alifatico-aromatico
JP2008539284A (ja) *	2005-04-29	2008-11-13	コルポラシオンドゥルコールポリテクニクドゥモンレアル	熱可塑性スターチ及び合成ポリマーのブレンド並びに製造方法
US20070082982A1 (en) *	2005-10-11	2007-04-12	The Procter & Gamble Company	Water stable compositions and articles comprising starch and methods of making the same
WO2007050560A2 (fr) *	2005-10-24	2007-05-03	Mgp Ingredients, Inc.	Composites thermoresistants a base d'amidon et de polyester et leurs procedes de fabrication
US20070129467A1 (en) *	2005-12-02	2007-06-07	Frederic Scheer	Bio based biodegradable polymer compositions and use of same
US7709595B2 (en) *	2006-07-28	2010-05-04	Eastman Chemical Company	Non-precipitating alkali/alkaline earth metal and aluminum solutions made with polyhydroxyl ether solvents
US20080027207A1 (en) *	2006-07-28	2008-01-31	Jason Christopher Jenkins	Non-precipitating alkali/alkaline earth metal and aluminum compositions made with mono-ol ether solvents
US7745368B2 (en) *	2006-07-28	2010-06-29	Eastman Chemical Company	Non-precipitating alkali/alkaline earth metal and aluminum compositions made with organic hydroxyacids
CA2659123C (fr) *	2006-07-28	2015-05-26	Biograde (Hong Kong) Pty Ltd	Composition de polymere biodegradable et melange maitre
US7709593B2 (en) *	2006-07-28	2010-05-04	Eastman Chemical Company	Multiple feeds of catalyst metals to a polyester production process
CN101506291B (zh) *	2006-08-04	2013-12-04	普朗蒂克科技有限公司	成型性的生物降解性聚合物
SA07280459B1 (ar)	2006-08-25	2011-07-20	بيورديو فارما إل. بي.	أشكال جرعة صيدلانية للتناول عن طريق الفم مقاومة للعبث تشتمل على مسكن شبه أفيوني
ITMI20061844A1 (it)	2006-09-27	2008-03-28	Novamont Spa	Composizioni biodegradabili a base di amido nanoparticellare
ITMI20061845A1 (it)	2006-09-27	2008-03-28	Novamont Spa	Composizioni biodegradabili polifasiche a base di amido
US8563677B2 (en)	2006-12-08	2013-10-22	Grupo Petrotemex, S.A. De C.V.	Non-precipitating alkali/alkaline earth metal and aluminum solutions made with diols having at least two primary hydroxyl groups
US8592641B2 (en) *	2006-12-15	2013-11-26	Kimberly-Clark Worldwide, Inc.	Water-sensitive biodegradable film
DE102007011485A1 (de) *	2007-03-07	2008-09-11	Grünenthal GmbH	Darreichungsform mit erschwertem Missbrauch
US20090043168A1 (en) *	2007-08-09	2009-02-12	Israel Ramos	Self-releasing tourniquet and method
US8329977B2 (en)	2007-08-22	2012-12-11	Kimberly-Clark Worldwide, Inc.	Biodegradable water-sensitive films
DE102007050770A1 (de) *	2007-10-22	2009-04-23	Biotec Biologische Naturverpackungen Gmbh & Co. Kg	Polymeres Material und Verfahren zu dessen Herstellung
CN101235156B (zh) *	2007-11-16	2011-04-20	江苏科技大学	一种聚乳酸/热塑性淀粉挤出吹塑薄膜及其生产方法与应用
US8227658B2 (en)	2007-12-14	2012-07-24	Kimberly-Clark Worldwide, Inc	Film formed from a blend of biodegradable aliphatic-aromatic copolyesters
US7678444B2 (en)	2007-12-17	2010-03-16	International Paper Company	Thermoformed article made from renewable polymer and heat-resistant polymer
US8383152B2 (en)	2008-01-25	2013-02-26	Gruenenthal Gmbh	Pharmaceutical dosage form
FR2927088B1 (fr) *	2008-02-01	2011-02-25	Roquette Freres	Compositions thermoplastiques a base d'amidon plastifie et procede de preparation de telles compositions.
FR2927084B1 (fr) *	2008-02-01	2011-02-25	Roquette Freres	Procede de preparation de compositions thermoplastiques a base d'amidon plastifie et compositions ainsi obtenues.
TWI524904B (zh)	2008-05-09	2016-03-11	歌林達股份有限公司	製備醫藥用固體劑型，尤指錠劑之方法，及製備固體劑型，尤指錠劑之前驅物之方法
FR2934272B1 (fr) *	2008-07-24	2013-08-16	Roquette Freres	Procede de preparation de compositions a base de matiere amylacee et de polymere synthetique.
IT1391097B1 (it) *	2008-08-05	2011-11-18	Novamont Spa	Contenitori biodegradabili colorati
KR20110095293A (ko) *	2008-11-06	2011-08-24	트리스타노 피티와이 리미티드	생분해성 폴리머 조성물
EP2380932B1 (fr)	2008-12-26	2018-03-14	Mitsubishi Chemical Corporation	Composition de résine, film, produit de type sac et procédé de fabrication de la composition de résine
WO2010105076A1 (fr) *	2009-03-11	2010-09-16	Nuvision Bioplastics, Llc	Mélange de résine biodégradable utilisé pour la fabrication de récipients biodégradables, récipients biodégradables et procédé de fabrication
CN101525487B (zh)	2009-03-31	2012-01-11	武汉华丽生物材料有限公司	一种可环境降解的复合材料及其制备方法
AU2009202397A1 (en) *	2009-06-16	2011-01-06	Because We Care Pty Ltd	Biodegradable Polymeric Compositions
NZ596668A (en)	2009-07-22	2013-09-27	Gruenenthal Chemie	Oxidation-stabilized tamper-resistant dosage form
JP5667183B2 (ja)	2009-07-22	2015-02-12	グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング	加熱溶融押出成型した制御放出性投与剤型
MX2012002751A (es) *	2009-09-03	2012-06-19	Co2Starch Pty Ltd	Composiciones de polimero/almidon termoplastico.
BR112012010007B1 (pt) *	2009-10-30	2021-04-06	Stichting Kennis Exploitatie Rb.	Composição biodegradável, artigo biodegradável e processo para fabricação de uma composição biodegradável
IT1399031B1 (it) *	2009-11-05	2013-04-05	Novamont Spa	Copoliestere alifatico-aromatico biodegradabile
IT1396597B1 (it)	2009-11-05	2012-12-14	Novamont Spa	Miscele di poliesteri biodegradabili
EP2509413A2 (fr)	2009-12-11	2012-10-17	Basf Se	Appâts pour rongeurs emballés dans une feuille biodégradable
US8586821B2 (en) *	2009-12-23	2013-11-19	Kimberly-Clark Worldwide, Inc.	Melt-processed films of thermoplastic cellulose and microbial aliphatic polyester
US8409677B2 (en) *	2010-01-20	2013-04-02	E I Du Pont De Nemours And Company	Biodegradable starch-containing blend
US8415021B2 (en) *	2010-01-20	2013-04-09	E I Du Pont De Nemours And Company	Biodegradable starch-containing composition with improved tear strength
EP2531176B1 (fr) *	2010-02-03	2016-09-07	Grünenthal GmbH	Préparation de composition pharmaceutique en poudre au moyen d'une extrudeuse
US20120016328A1 (en) *	2010-07-19	2012-01-19	Bo Shi	Biodegradable films
MX2013002293A (es)	2010-09-02	2013-05-09	Gruenenthal Gmbh	Forma de dosificacion resistente a alteracion que comprende un polimero anionico.
ES2486791T3 (es)	2010-09-02	2014-08-19	Grünenthal GmbH	Forma de dosificación resistente a la manipulación que comprende una sal inorgánica
TWI417333B (zh) *	2010-09-06	2013-12-01	Ind Tech Res Inst	澱粉基熱塑性複合材料
US8907155B2 (en)	2010-11-19	2014-12-09	Kimberly-Clark Worldwide, Inc.	Biodegradable and flushable multi-layered film
FR2969627B1 (fr) *	2010-12-27	2014-10-17	Arkema France	Compositions a base de copolyether bloc amides, de copolyether bloc esters, de polyolefines fonctionnalisees et d'amidon pour des applications de film imper respirants
KR101406989B1 (ko) *	2011-01-18	2014-06-13	에스케이이노베이션 주식회사	다층필름
CN102321249B (zh)	2011-06-30	2013-01-16	无锡碧杰生物材料科技有限公司	一种热塑性淀粉和生物降解聚酯/淀粉复合材料及其制备
US8933162B2 (en)	2011-07-15	2015-01-13	Saudi Basic Industries Corporation	Color-stabilized biodegradable aliphatic-aromatic copolyesters, methods of manufacture, and articles thereof
US8877862B2 (en)	2011-07-15	2014-11-04	Saudi Basic Industries Corporation	Method for color stabilization of poly(butylene-co-adipate terephthalate
US9334360B2 (en)	2011-07-15	2016-05-10	Sabic Global Technologies B.V.	Color-stabilized biodegradable aliphatic-aromatic copolyesters, methods of manufacture, and articles thereof
WO2013011977A1 (fr) *	2011-07-21	2013-01-24	Dic株式会社	Composition à base de résine de polycarbonate et moulage en résine à base de celle-ci
EA201400172A1 (ru)	2011-07-29	2014-06-30	Грюненталь Гмбх	Устойчивая к разрушению таблетка, которая обеспечивает немедленное высвобождение лекарственного средства
PE20141650A1 (es)	2011-07-29	2014-11-22	Gruenenthal Chemie	Tableta a prueba de alteracion que proporciona liberacion inmediata del farmaco
US8946345B2 (en)	2011-08-30	2015-02-03	Saudi Basic Industries Corporation	Method for the preparation of (polybutylene-co-adipate terephthalate) through the in situ phosphorus containing titanium based catalyst
US20150265536A1 (en) *	2011-12-09	2015-09-24	Purdue Pharma L.P.	Pharmaceutical dosage forms comprising poly(epsilon-caprolactone) and polyethylene oxide
JP5936953B2 (ja) *	2011-12-12	2016-06-22	第一工業製薬株式会社	ポリ乳酸樹脂組成物およびその樹脂成形体
US9718258B2 (en)	2011-12-20	2017-08-01	Kimberly-Clark Worldwide, Inc.	Multi-layered film containing a biopolymer
US9327438B2 (en)	2011-12-20	2016-05-03	Kimberly-Clark Worldwide, Inc.	Method for forming a thermoplastic composition that contains a plasticized starch polymer
WO2013127831A1 (fr)	2012-02-28	2013-09-06	Grünenthal GmbH	Forme pharmaceutique inviolable comprenant un composé pharmacologiquement actif et un polymère anionique
US8895660B2 (en)	2012-03-01	2014-11-25	Saudi Basic Industries Corporation	Poly(butylene-co-adipate terephthalate), method of manufacture, and uses thereof
US9034983B2 (en)	2012-03-01	2015-05-19	Saudi Basic Industries Corporation	Poly(butylene-co-adipate terephthalate), method of manufacture and uses thereof
US20130253102A1 (en) *	2012-03-26	2013-09-26	Sung-Yuan LIU	Biodegradable plastic material
US8901243B2 (en)	2012-03-30	2014-12-02	Saudi Basic Industries Corporation	Biodegradable aliphatic-aromatic copolyesters, methods of manufacture, and articles thereof
ES2692944T3 (es)	2012-04-18	2018-12-05	Grünenthal GmbH	Forma de dosificación farmacéutica resistente a la manipulación y resistente a la descarga rápida de la dosis
US10064945B2 (en)	2012-05-11	2018-09-04	Gruenenthal Gmbh	Thermoformed, tamper-resistant pharmaceutical dosage form containing zinc
GB201217207D0 (en) *	2012-09-26	2012-11-07	Biome Bioplastics Ltd	Bio-resins
WO2014075998A1 (fr)	2012-11-15	2014-05-22	Basf Se	Mélange polyester biodégradable
US9056979B2 (en)	2012-11-15	2015-06-16	Basf Se	Biodegradable polyester mixture
GB201300538D0 (en) *	2013-01-11	2013-02-27	Norner As	Polycarbonates
US10829621B2 (en) *	2013-01-11	2020-11-10	Monosol, Llc	Edible water-soluble film
CN103122133B (zh) *	2013-03-19	2015-02-11	宁波家塑生物材料科技有限公司	一种聚乳酸/植物多糖环保型复合材料及其制备方法
PL2784114T3 (pl)	2013-03-26	2016-04-29	Sa Minera Catalano Aragonesa	Biodegradowalny polimer pochodzenia naturalnego
US9737490B2 (en)	2013-05-29	2017-08-22	Grünenthal GmbH	Tamper resistant dosage form with bimodal release profile
BR112015026549A2 (pt)	2013-05-29	2017-07-25	Gruenenthal Gmbh	forma de dosagem à prova de violação contendo uma ou mais partículas
AU2014289187B2 (en)	2013-07-12	2019-07-11	Grunenthal Gmbh	Tamper-resistant dosage form containing ethylene-vinyl acetate polymer
WO2015052876A1 (fr) *	2013-10-11	2015-04-16	株式会社カネカ	Composition de résine polyester aliphatique et corps moulé en résine polyester aliphatique
ES2869024T3 (es) *	2013-11-08	2021-10-22	Hollister Inc	Catéteres oleófilos lubricados
AU2014356581C1 (en)	2013-11-26	2020-05-28	Grunenthal Gmbh	Preparation of a powdery pharmaceutical composition by means of cryo-milling
DE102014223786A1 (de)	2013-12-10	2015-06-11	Basf Se	Polymermischung für Barrierefilm
MX2016014738A (es)	2014-05-12	2017-03-06	Gruenenthal Gmbh	Formulacion en capsula de liberacion inmediata resistente a alteraciones que comprende tapentadol.
CN106456550A (zh)	2014-05-26	2017-02-22	格吕伦塔尔有限公司	避免乙醇剂量倾泻的多颗粒
BR112017021475A2 (pt)	2015-04-24	2018-07-10	Gruenenthal Gmbh	forma de dosagem resistente à adulteração (tamper) com liberação imediata e resistência contra extração de solvente
US11111363B2 (en)	2015-06-30	2021-09-07	BiologiQ, Inc.	Articles formed with renewable and/or sustainable green plastic material and carbohydrate-based polymeric materials lending increased strength and/or biodegradability
US11926940B2 (en)	2015-06-30	2024-03-12	BiologiQ, Inc.	Spunbond nonwoven materials and fibers including starch-based polymeric materials
US11674018B2 (en)	2015-06-30	2023-06-13	BiologiQ, Inc.	Polymer and carbohydrate-based polymeric material blends with particular particle size characteristics
US11111355B2 (en)	2015-06-30	2021-09-07	BiologiQ, Inc.	Addition of biodegradability lending additives to plastic materials
US11046840B2 (en)	2015-06-30	2021-06-29	BiologiQ, Inc.	Methods for lending biodegradability to non-biodegradable plastic materials
US11149144B2 (en) *	2015-06-30	2021-10-19	BiologiQ, Inc.	Marine biodegradable plastics comprising a blend of polyester and a carbohydrate-based polymeric material
US11926929B2 (en)	2015-06-30	2024-03-12	Biologiq, Inc	Melt blown nonwoven materials and fibers including starch-based polymeric materials
US11674014B2 (en)	2015-06-30	2023-06-13	BiologiQ, Inc.	Blending of small particle starch powder with synthetic polymers for increased strength and other properties
US11879058B2 (en)	2015-06-30	2024-01-23	Biologiq, Inc	Yarn materials and fibers including starch-based polymeric materials
US11359088B2 (en)	2015-06-30	2022-06-14	BiologiQ, Inc.	Polymeric articles comprising blends of PBAT, PLA and a carbohydrate-based polymeric material
US11051504B2 (en)	2015-07-13	2021-07-06	Basf Corporation	Pest control and detection system with conductive bait matrix
US10085435B2 (en)	2015-07-13	2018-10-02	Basf Corporation	Pest control and detection system with conductive bait matrix
CA2998259A1 (fr)	2015-09-10	2017-03-16	Grunenthal Gmbh	Protection contre un surdosage par voie orale a l'aide de formulations a liberation immediate dissuasives d'abus
EP3394164A1 (fr) *	2015-12-22	2018-10-31	Rhodia Acetow GmbH	Nouvelles compositions plastifiées comprenant de l'acétate de cellulose
JP2020502355A (ja)	2016-12-22	2020-01-23	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	フランジカルボン酸含有ポリエステル
CN107129672A (zh) *	2017-06-02	2017-09-05	苏州市雄林新材料科技有限公司	一种画板用易擦拭tpu薄膜及其制备方法
MX2020000229A (es)	2017-07-07	2020-08-17	Basf Corp	Sistema de monitoreo de plagas con electrodos conductores.
KR101875603B1 (ko) *	2017-09-19	2018-07-06	양태권	토양개량 및 비료 기능을 가지는 생분해성 농업용 멀칭필름용 수지 조성물 및 이를 이용하여 제조된 생분해성 농업용 멀칭필름
FR3075215B1 (fr)	2017-12-19	2020-11-20	Lactips	Materiau thermoplastique biodegradable a base de caseine et/ou de caseinate
CN109535490B (zh) *	2018-11-26	2021-01-12	四川理工学院	一种用于填充改性可降解高分子材料的淀粉母料及其制备方法
CN109553809B (zh) *	2018-11-26	2021-01-12	四川理工学院	一种高韧性pbs/淀粉复合材料及其制备方法
PT3891208T (pt)	2018-12-06	2023-05-02	Basf Se	Processo para produzir um (co) poliéster
WO2020156970A1 (fr)	2019-01-30	2020-08-06	Basf Se	Procédé de production de mélanges d'amidon
JP7657444B2 (ja) *	2020-02-10	2025-04-07	株式会社コバヤシ	樹脂組成物及びその製造方法、並びに可塑化澱粉及びその製造方法
EP3995534B1 (fr)	2020-11-10	2025-10-22	Gaia Plas Berhad	Résine de polymère et ses utilisations
ES2897213B2 (es) *	2021-02-19	2022-11-30	Univ Alicante	Procedimiento de obtencion de un material plastificado. el material plastificado obtenido y su uso
KR102464416B1 (ko) *	2022-03-17	2022-11-10	대로방수화학 주식회사	일액형 방수제 제조방법 및 그에 의하여 제조되는 일액형 방수제
IT202200012215A1 (it)	2022-06-09	2023-12-09	All Packaging S R L	Materiale plastico biodegradabile riciclato e sistema di produzione dello stesso
CN115260542B (zh) *	2022-07-11	2024-10-29	湖北宜化降解新材料有限公司	可降解聚合物/淀粉母粒的制备方法
WO2024074562A1 (fr)	2022-10-06	2024-04-11	Basf Se	Mélange de polymères thermoplastiques et son utilisation
CN119176925A (zh) *	2024-11-22	2024-12-24	道一高分子聚合物(宁波)有限公司	一种tpu塑胶跑道材料的制备方法及应用

Family Cites Families (52)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3843708A (en) *	1969-01-17	1974-10-22	Union Carbide Corp	Extended polylactone diol compositions
US4055534A (en) *	1975-11-14	1977-10-25	Horizons Incorporated, A Division Of Horizons Research Incorporated	Upgraded aromatic polyester material in powder form
JPS5939096B2 (ja) *	1978-06-27	1984-09-20	ダイセル化学工業株式会社	ソルビン酸を含む溶融物被覆製剤
IE66735B1 (en)	1988-11-03	1996-02-07	Biotec Biolog Naturverpack	Thermoplastically workable starch and a method for the manufacture thereof
IL93620A0 (en) *	1989-03-09	1990-12-23	Butterfly Srl	Biodegradable articles based on starch and process for producing them
IT1232909B (it)	1989-08-07	1992-03-05	Butterfly Srl	Composizione polimerica per la produzione di articoli di materiale plastico biodegradabile comprendente amido destrutturato e copolimero di etilene
US5219646A (en)	1990-05-11	1993-06-15	E. I. Du Pont De Nemours And Company	Polyester blends and their use in compostable products such as disposable diapers
ATE199383T1 (de)	1990-11-30	2001-03-15	Eastman Chem Co	Aliphatisch-aromatische copolyester
IT1245408B (it)	1991-02-20	1994-09-20	Butterfly Srl	Composizioni polimeriche biodegradabili a base di amido e di polimero termoplastico
US5292782A (en)	1991-02-20	1994-03-08	Novamont S.P.A.	Biodegradable polymeric compositions based on starch and thermoplastic polymers
IT1245485B (it)	1991-05-03	1994-09-20	Butterfly Srl	Membrane permselettive e loro impiego
US5412005A (en)	1991-05-03	1995-05-02	Novamont S.P.A.	Biodegradable polymeric compositions based on starch and thermoplastic polymers
JP2527523B2 (ja)	1991-05-03	1996-08-28	ノバモント・ソシエタ・ペル・アチオニ	デンプンと熱可塑性高分子をベ―スにした生分解性高分子組成物
IT1256693B (it)	1992-03-10	1995-12-12	Novamont Spa	Composizione polimerica amidacea filmabile, ed articoli sagomati, particolarmente film e foglie ottenibili da tale composizione, aventi elevato effetto barriera e procedimento relativo.
DE4117628C3 (de) *	1991-05-29	1999-02-11	Inventa Ag	Verfahren und Vorrichtung zur Herstellung von Stärkeschmelze sowie nach diesem Verfahren erhältliche Produkte
PL173320B1 (pl) *	1991-06-26	1998-02-27	Procter & Gamble	Folia ulegajaca rozkładowi biologicznemu i nieprzenikalna dla płynów
FR2682110B1 (fr)	1991-10-02	1995-05-24	Atta	Ligands amphiphiles perfluoroalkyles leurs complexes metalliques et leurs utilisations dans des preparations a usage therapeutique.
IT1250045B (it)	1991-11-07	1995-03-30	Butterfly Srl	Procedimento per la produzione di alcool polivinilico plastificato e suo impiego per la preparazione di composizioni termoplastiche biodegradabili a base di amido.
IT1250901B (it) *	1991-12-12	1995-04-21	Novamont Spa	Articoli biodegradabili a base di amido.
US6277899B1 (en) *	1992-08-03	2001-08-21	Novamont S.P.A.	Biodegradable polymeric composition
IT1256914B (it) *	1992-08-03	1995-12-27	Novamont Spa	Composizione polimerica biodegradabile.
US5312850A (en) *	1993-01-04	1994-05-17	National Starch And Chemical Investment Holding Corporation	Polylactide and starch containing hot melt adhesive
DE4237535C2 (de)	1992-11-06	2000-05-25	Biotec Biolog Naturverpack	Biologisch abbaubare Polymermischung, ein Verfahren und eine Folie
US5844023A (en)	1992-11-06	1998-12-01	Bio-Tec Biologische Naturverpackungen Gmbh	Biologically degradable polymer mixture
US5321088A (en)	1992-11-09	1994-06-14	Mobil Oil Corporation	Graft copolymers of polyethylene and polycaprolactone
US5374671A (en)	1993-02-16	1994-12-20	The Goodyear Tire & Rubber Company	Hydrophilic polymer composite and product containing same
US5462983A (en) *	1993-07-27	1995-10-31	Evercorn, Inc.	Biodegradable moldable products and films comprising blends of starch esters and polyesters
DE4327024A1 (de)	1993-08-12	1995-02-16	Bayer Ag	Thermoplastisch verarbeitbare und biologisch abbaubare aliphatische Polyesteramide
FI99125C (fi)	1993-12-31	1997-10-10	Neste Oy	Polylaktidikoostumus
US5500465A (en)	1994-03-10	1996-03-19	Board Of Trustees Operating Michigan State University	Biodegradable multi-component polymeric materials based on unmodified starch-like polysaccharides
US5650473A (en) *	1994-07-22	1997-07-22	National Starch And Chemical Investment Holding Corporation	Methods for making styrene copolymers and uses thereof
JP3420845B2 (ja) *	1994-09-14	2003-06-30	日本合成化学工業株式会社	樹脂分散液組成物及びその用途
US5552461A (en)	1994-12-30	1996-09-03	Environmental Packing L.P.	Composition and method for improving the extrusion characteristics of aqueous starch-polymer mixtures
IT1272871B (it) *	1995-01-10	1997-07-01	Novamont Spa	Composizioni termoplastiche compredenti amido ed altre componenti di origine naturale
DE19500756A1 (de)	1995-01-13	1996-07-18	Basf Ag	Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper
DE19500754A1 (de)	1995-01-13	1996-07-18	Basf Ag	Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper
DE19500755A1 (de)	1995-01-13	1996-07-18	Basf Ag	Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper
DE19500757A1 (de)	1995-01-13	1996-07-18	Basf Ag	Biologisch abbaubare Polymere, Verfahren zu deren Herstellung sowie deren Verwendung zur Herstellung bioabbaubarer Formkörper
JP3107830B2 (ja)	1995-04-07	2000-11-13	ビオ−テックビオロギッシェナトゥーアフェアパックンゲンゲゼルシャフトミットベシュレンクテルハフツングウントコンパニーコマンディートゲゼルシャフト	生物学的に分解可能なポリマー混合物
US5773146A (en) *	1995-06-05	1998-06-30	Ppg Industries, Inc.	Forming size compositions, glass fibers coated with the same and fabrics woven from such coated fibers
EP0758641B1 (fr)	1995-08-11	2000-08-30	Daicel Chemical Industries, Ltd.	Composition d'esters gras de polyglycérine, son procédé de préparation, procédé de préparation d'une composition d'esters gras de polyglycérine très pure, une composition d'esters de polyglycérine gras très pure, un additif alimentaire, une composition de résine et une composition pour cosmétiques ou détergents
US5861461A (en) *	1995-12-06	1999-01-19	Yukong Limited	Biodegradable plastic composition, method for preparing thereof and product prepared therefrom
US5756194A (en) *	1996-01-25	1998-05-26	The United States Of America, As Represented By The Secretary Of Agriculture	Enhanced water resistance of starch-based materials
US5821286A (en) *	1996-05-24	1998-10-13	The United States Of America As Represented By The Secretary Of The Agriculture	Biodegradable polyester and natural polymer compositions and films therefrom
US6025417A (en) *	1996-02-28	2000-02-15	Biotechnology Research & Development Corp.	Biodegradable polyester compositions with natural polymers and articles thereof
US5773983A (en) *	1996-07-17	1998-06-30	Rpi, Inc.	Electrical transfer switch and related method
EP0950689B1 (fr) *	1996-11-05	2004-10-06	NOVAMONT S.p.A.	Compositions polymériques biodégradables contenant de l'amidon et un polymère thermoplastique
US5834533A (en)	1996-11-20	1998-11-10	Phillips Petroleum Company	Stable liquid suspension compositions
ITTO980524A1 (it) *	1998-06-17	1999-12-17	Novamont Spa	Composizioni contenenti amido aventi elevata resistenza all'invecchiam ento.
IT1303553B1 (it) *	1998-09-01	2000-11-14	Novamont Spa	Composizioni biodegradabili comprendenti amido ed esteri di cellulosa.
IT1305576B1 (it) *	1998-09-22	2001-05-09	Novamont Spa	Polimeri a carattere idrofobico caricati con complessi dell'amido.
ITMI20061845A1 (it) *	2006-09-27	2008-03-28	Novamont Spa	Composizioni biodegradabili polifasiche a base di amido

1997
- 1997-11-05 EP EP99113031A patent/EP0950689B1/fr not_active Expired - Lifetime
- 1997-11-05 WO PCT/EP1997/006103 patent/WO1998020073A2/fr not_active Ceased
- 1997-11-05 EP EP99113033A patent/EP0947559B1/fr not_active Expired - Lifetime
- 1997-11-05 DE DE69730852T patent/DE69730852T2/de not_active Expired - Lifetime
- 1997-11-05 IL IL12974597A patent/IL129745A0/xx active IP Right Grant
- 1997-11-05 DK DK99113033T patent/DK0947559T3/da active
- 1997-11-05 AT AT97950097T patent/ATE277124T1/de active
- 1997-11-05 AT AT99113033T patent/ATE280803T1/de active
- 1997-11-05 KR KR1019997004001A patent/KR100329588B1/ko not_active Expired - Fee Related
- 1997-11-05 AU AU53174/98A patent/AU724397B2/en not_active Expired
- 1997-11-05 US US09/297,733 patent/US7176251B1/en not_active Expired - Fee Related
- 1997-11-05 EP EP97950097A patent/EP0937120B1/fr not_active Expired - Lifetime
- 1997-11-05 DE DE69731396T patent/DE69731396C5/de not_active Expired - Lifetime
- 1997-11-05 CN CN97181070A patent/CN1104467C/zh not_active Expired - Lifetime
- 1997-11-05 BR BR9712882-1A patent/BR9712882A/pt not_active IP Right Cessation
- 1997-11-05 AT AT99113031T patent/ATE278737T1/de not_active IP Right Cessation
- 1997-11-05 ES ES99113033T patent/ES2229591T3/es not_active Expired - Lifetime
- 1997-11-05 CA CA2270362A patent/CA2270362C/fr not_active Expired - Lifetime
- 1997-11-05 EP EP10183869.6A patent/EP2270093A3/fr not_active Withdrawn
- 1997-11-05 EP EP05001336A patent/EP1526156A3/fr not_active Withdrawn
- 1997-11-05 DE DE69731114T patent/DE69731114T2/de not_active Expired - Lifetime
- 1997-11-05 HU HU0000335A patent/HU229197B1/hu unknown
- 1997-11-05 AT AT99113032T patent/ATE287928T1/de not_active IP Right Cessation
- 1997-11-05 EP EP99113032A patent/EP0950690B1/fr not_active Expired - Lifetime
- 1997-11-05 DE DE69732371T patent/DE69732371T2/de not_active Expired - Lifetime
- 1997-11-05 DK DK99113031T patent/DK0950689T3/da active
- 1997-11-05 JP JP52105598A patent/JP4034357B2/ja not_active Expired - Fee Related
1999
- 1999-05-03 IL IL129745A patent/IL129745A/en not_active IP Right Cessation
- 1999-05-04 NO NO19992159A patent/NO335963B1/no not_active IP Right Cessation
2007
- 2007-01-25 US US11/657,799 patent/US7956107B2/en not_active Expired - Fee Related
- 2007-01-25 US US11/657,857 patent/US8410199B2/en not_active Expired - Fee Related
- 2007-08-13 JP JP2007211032A patent/JP2007321162A/ja active Pending
2008
- 2008-01-17 IL IL188860A patent/IL188860A/en not_active IP Right Cessation
2011
- 2011-10-18 JP JP2011228798A patent/JP2012036403A/ja active Pending

Also Published As

Publication number	Publication date
EP1526156A2 (fr)	2005-04-27
CA2270362A1 (fr)	1998-05-14
US20070129468A1 (en)	2007-06-07
NO335963B1 (no)	2015-03-30
EP0937120A2 (fr)	1999-08-25
EP2270093A3 (fr)	2013-10-30
DE69732371D1 (de)	2005-03-03
HU229197B1 (en)	2013-09-30
ATE287928T1 (de)	2005-02-15
JP2007321162A (ja)	2007-12-13
DE69732371T2 (de)	2005-06-30
EP0950689A3 (fr)	2000-06-14
DE69731396C5 (de)	2013-10-31
IL188860A (en)	2010-05-17
DE69731114D1 (de)	2004-11-11
CN1242032A (zh)	2000-01-19
EP0950690A2 (fr)	1999-10-20
AU5317498A (en)	1998-05-29
CN1104467C (zh)	2003-04-02
US8410199B2 (en)	2013-04-02
KR100329588B1 (ko)	2002-03-21
HUP0000335A2 (hu)	2000-06-28
DK0950689T3 (da)	2005-02-07
DK0947559T3 (da)	2005-02-14
BR9712882A (pt)	2000-02-01
HUP0000335A3 (en)	2002-10-28
IL129745A (en)	2008-04-13
EP0947559B1 (fr)	2004-10-27
ATE278737T1 (de)	2004-10-15
DE69730852T2 (de)	2005-09-22
DE69731396D1 (de)	2004-12-02
ATE280803T1 (de)	2004-11-15
US7956107B2 (en)	2011-06-07
AU724397B2 (en)	2000-09-21
NO992159L (no)	1999-05-04
JP4034357B2 (ja)	2008-01-16
NO992159D0 (no)	1999-05-04
ATE277124T1 (de)	2004-10-15
DE69731114T2 (de)	2006-02-23
IL129745A0 (en)	2000-02-29
US7176251B1 (en)	2007-02-13
EP0950689A2 (fr)	1999-10-20
EP0950690A3 (fr)	2000-09-06
EP0950690B1 (fr)	2005-01-26
WO1998020073A2 (fr)	1998-05-14
US20070123612A1 (en)	2007-05-31
JP2012036403A (ja)	2012-02-23
JP2000509427A (ja)	2000-07-25
IL188860A0 (en)	2008-04-13
EP1526156A3 (fr)	2005-07-27
DE69730852D1 (de)	2004-10-28
EP0947559A3 (fr)	2000-06-14
EP0947559A2 (fr)	1999-10-06
CA2270362C (fr)	2011-12-13
EP2270093A2 (fr)	2011-01-05
DE69731396T2 (de)	2005-03-24
WO1998020073A3 (fr)	1998-08-06
EP0950689B1 (fr)	2004-10-06
EP0937120B1 (fr)	2004-09-22
KR20000053078A (ko)	2000-08-25

Publication	Publication Date	Title
ES2229591T3 (es)	2005-04-16	Composiciones polimericas biodegradables que comprenden almidon y un polimero termoplastico.
ES2540532T3 (es)	2015-07-10	Mezcla madre y composición polimérica
EP0722980B1 (fr)	2001-11-14	Compositions thermoplastiques comprenant de l'amidon et des autres composants d'origine naturelle
KR100272484B1 (ko)	2000-11-15	생분해성 중합체 조성물
ES2310913T3 (es)	2009-01-16	Copoliester alifatico-aromatico biodegradable.
ES2905188T3 (es)	2022-04-07	Almidón termoplástico
ES2768873T3 (es)	2020-06-23	Mezclas de poliésteres biodegradables con por lo menos un polímero de origen natural
US20020028857A1 (en)	2002-03-07	Compostable, degradable plastic compositions and articles thereof
JP7360450B2 (ja)	2023-10-12	ポリエステル系樹脂組成物の製造方法
ES2950810T3 (es)	2023-10-13	Almidón termoplástico
ITTO960890A1 (it)	1998-05-05	Composizioni polimeriche eterofasiche comprendenti amido e un polimero temoplastico.